Tmem45a Variant Search Result - Rat Genome Database

Advanced Search (OLGA)

Variants search result for All species
(View Results for all Objects and Ontologies)

27 records found for search term Tmem45a

Refine Term:

Sort By:

Export

CSV

TAB

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8577673	CV112050	single nucleotide variant	NM_018004.1(TMEM45A):c.-4+8899A>G	Lung cancer [RCV000092573]	uncertain significance	3	100501827	100501827	Human		name
8625439	CV80562	single nucleotide variant	NM_018004.1(TMEM45A):c.201G>A (p.Gly67=)	Malignant melanoma [RCV000060639]	not provided	3	100556770	100556770	Human		name
156331101	CV2220480	single nucleotide variant	NM_018004.3(TMEM45A):c.63G>C (p.Trp21Cys)	not specified [RCV004097710]	uncertain significance	3	100555274	100555274	Human		name
401860868	CV2772284	single nucleotide variant	NM_018004.3(TMEM45A):c.73A>T (p.Ser25Cys)	not specified [RCV004353306]	likely benign	3	100555284	100555284	Human		name
405771315	CV3346568	single nucleotide variant	NM_018004.3(TMEM45A):c.35C>A (p.Thr12Asn)	not specified [RCV004470339]	uncertain significance	3	100555246	100555246	Human		name
401888302	CV2788285	single nucleotide variant	NM_018004.3(TMEM45A):c.182C>A (p.Ala61Asp)	not specified [RCV004352874]	uncertain significance	3	100555393	100555393	Human		name
597800429	CV3610550	single nucleotide variant	NM_018004.3(TMEM45A):c.139T>A (p.Tyr47Asn)	not specified [RCV004880233]	uncertain significance	3	100555350	100555350	Human		name
598252550	CV3913932	single nucleotide variant	NM_018004.3(TMEM45A):c.122G>C (p.Gly41Ala)	not specified [RCV005278105]	uncertain significance	3	100555333	100555333	Human		name
8625438	CV80561	single nucleotide variant	NM_018004.1(TMEM45A):c.200G>A (p.Gly67Glu)	Malignant melanoma [RCV000060638]	not provided	3	100556769	100556769	Human		name
155924352	CV2277088	single nucleotide variant	NM_018004.3(TMEM45A):c.647A>C (p.Glu216Ala)	not specified [RCV004142740]	uncertain significance	3	100568880	100568880	Human		name
156121723	CV2354276	single nucleotide variant	NM_018004.3(TMEM45A):c.478G>A (p.Val160Ile)	not specified [RCV004206698]	likely benign	3	100558479	100558479	Human		name
329353926	CV2436653	single nucleotide variant	NM_018004.3(TMEM45A):c.439A>G (p.Met147Val)	not specified [RCV004258027]	uncertain significance	3	100558440	100558440	Human		name
329393474	CV2467011	single nucleotide variant	NM_018004.3(TMEM45A):c.548G>T (p.Arg183Leu)	not specified [RCV004282756]	uncertain significance	3	100558549	100558549	Human		name
401772097	CV2708120	single nucleotide variant	NM_018004.3(TMEM45A):c.706G>A (p.Val236Ile)	not specified [RCV004311495]	likely benign	3	100568939	100568939	Human		name
401737586	CV2718143	single nucleotide variant	NM_018004.3(TMEM45A):c.619G>A (p.Gly207Ser)	not specified [RCV004315851]	uncertain significance	3	100568852	100568852	Human		name
401769419	CV2735021	single nucleotide variant	NM_018004.3(TMEM45A):c.745T>G (p.Ser249Ala)	not specified [RCV004333721]	uncertain significance	3	100576935	100576935	Human		name
401876447	CV2785898	single nucleotide variant	NM_018004.3(TMEM45A):c.805C>A (p.Gln269Lys)	not specified [RCV004365417]	uncertain significance	3	100576995	100576995	Human		name
405771324	CV3346569	single nucleotide variant	NM_018004.3(TMEM45A):c.695C>A (p.Thr232Asn)	not specified [RCV004470340]	uncertain significance	3	100568928	100568928	Human		name
405771331	CV3346570	single nucleotide variant	NM_018004.3(TMEM45A):c.782T>G (p.Leu261Arg)	not specified [RCV004470341]	uncertain significance	3	100576972	100576972	Human		name
405771337	CV3346571	single nucleotide variant	NM_018004.3(TMEM45A):c.800G>A (p.Arg267Gln)	not specified [RCV004470342]	uncertain significance	3	100576990	100576990	Human		name
407458802	CV3482761	single nucleotide variant	NM_018004.3(TMEM45A):c.583T>G (p.Phe195Val)	not specified [RCV004686944]	uncertain significance	3	100558584	100558584	Human		name
407526772	CV3482762	single nucleotide variant	NM_018004.3(TMEM45A):c.436G>A (p.Glu146Lys)	not specified [RCV004679760]	uncertain significance	3	100558437	100558437	Human		name
407526781	CV3482765	single nucleotide variant	NM_018004.3(TMEM45A):c.770C>T (p.Ser257Leu)	not specified [RCV004679763]	uncertain significance	3	100576960	100576960	Human		name
597800427	CV3610549	single nucleotide variant	NM_018004.3(TMEM45A):c.521G>A (p.Arg174Gln)	not specified [RCV004880232]	uncertain significance	3	100558522	100558522	Human		name
597800431	CV3610551	single nucleotide variant	NM_018004.3(TMEM45A):c.500C>A (p.Ala167Asp)	not specified [RCV004880234]	uncertain significance	3	100558501	100558501	Human		name
598252543	CV3913930	single nucleotide variant	NM_018004.3(TMEM45A):c.433C>T (p.Arg145Trp)	not specified [RCV005278104]	uncertain significance	3	100558434	100558434	Human		name
598227022	CV3913931	single nucleotide variant	NM_018004.3(TMEM45A):c.424A>G (p.Thr142Ala)	not specified [RCV005294518]	uncertain significance	3	100558425	100558425	Human		name

Gene Annotator (Functional Annotation) unavailable	Gene Annotator (Annotation Distribution) unavailable	Variant Visualizer (Genomic Variants) unavailble Variant Visualizer (Genomic Variants) unavailable
Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

InterViewer (Protein-Protein Interactions) unavailable	Gviewer (Genome Viewer) unavailable	Variant Visualizer (Damaging Variants) unavailble Variant Visualizer (Damaging Variants) unavailable
InterViewer (Protein-Protein Interactions)	GViewer (Genome Viewer)	Variant Visualizer (Damaging Variants)

Gene Annotator (Annotation Comparison) unavailable	OLGA (Gene List Generator) unavailable
Gene Annotator (Annotation Comparison)	OLGA (Gene List Generator)	Excel (Download)

MOET (Multi-Ontology Enrichement) unavailable	GOLF (Gene-Ortholog Location Finder) unavailable
MOET (Multi-Ontology Enrichement)	GOLF (Gene-Ortholog Location Finder)

Create Name:

Description:

Send us a Message